منابع مشابه
Mycosis fungoides and Sezary syndrome.
YCOSIS FUNGOIDES (MF) is an uncommon, indoM lent T-cell lymphoma first described by Alibert' in the early 1800s. It primarily involves the skin at early stages of the disease, with plaques being the typical feature. After a variable period of time, it may progress with development of cutaneous tumors and spread to visceral sites and lymph nodes (LNs).* SBzary syndrome (SS) is an erythrodermic v...
متن کاملMycosis fungoides and Sézary syndrome.
Mycosis fungoides and Sézary syndrome are the most common of the cutaneous T-cell lymphomas, which are a heterogeneous group of neoplasms that affect the skin as a primary site. Although the aetiologies of mycosis fungoides and Sézary syndrome are unknown, important insights have been gained in the immunological and genetic perturbations that are associated with these diseases. Unlike some B-ce...
متن کاملDiagnostics in mycosis fungoides and Sezary syndrome.
AIM The aim of this paper was to present diagnostic methods helping in the recognition of mycosis fungoides (MF) and Sezary syndrome (SS). BACKGROUND Mycosis fungoides is the most common form of primary cutaneous T-cell lymphomas. It is characterized by a distinctive long-term course and malignant T-cell proliferation. MF diagnosis is not easy, mainly due to the atypical clinical presentation...
متن کاملIncreased serum neopterin levels in mycosis fungoides and Sézary syndrome.
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متن کاملTransformation of Mycosis Fungoides/Sezary Syndrome: Clinical Characteristics and Prognosis
OBJECTIVE Transformed mycosis fungoides (T-MF) is a rare variant of MF with an aggressive course. In this study, we aimed to describe characteristics of MF/Sezary syndrome (SS) patients with transformation. MATERIALS AND METHODS Patients diagnosed with T-MF among MF/SS patients between 2000 and 2014 in a tertiary single center were evaluated retrospectively. Demographic data, clinical data, l...
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ژورنال
عنوان ژورنال: Atlas of Genetics and Cytogenetics in Oncology and Haematology
سال: 2011
ISSN: 1768-3262
DOI: 10.4267/2042/38218